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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467507Generated: October 30, 2026

Aminoacetaldehyde dimethyl acetal → HCID 58497247, compound

https://huagongshe.com/reaction/467507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 59534515HCID 59534515—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58497247HCID 58497247—

Reaction Steps

906 mg (4.73 mmol) of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDCI) are added to a solution of 1.24 g (3.64 mmol) of 3-[3-(3,5-difluorophenyl)-6-oxo-6H-pyridazin-1-ylmethyl]benzoic acid (prepared in accordance with WO 2008/017361), 382 mg (3.64 mmol) of aminoacetaldehyde dimethyl acetal and 557 mg (3.64 mmol) of 1-hydroxybenzotriazole hydrate (HOBt) in 14 ml of DMF, and the mixture is stirred overnight at room temperature. Water is added to the reaction mixture. The precipitate formed is filtered off with suction, washed with water and dried in vacuo, giving 3-[3-(3,5-difluorophenyl)-6-oxo-6H-pyridazin-1-ylmethyl]-N-(2,2-dimethoxyethyl)benzamide as colourless crystals; ESI 430.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623870B2
Source datasetuspto-grants-2014_01
ORD IDord-e3e1b89240184e01909610caff05b0da
Source noteuspto-grants-2014_01